ANGPTL4 silencing via antisense oligonucleotides reduces plasma triglycerides and glucose in mice without causing

Mingjuan Deng1, Elda Kutrolli2, Anne Sadewasser3

  • 1Nutrition, Metabolism and Genomics Group, Division of Human Nutrition and Health, Wageningen University, Wageningen, the Netherlands.

Insights

Silencing Angiopoietin-like 4 (ANGPTL4) with antisense oligonucleotides (ASOs) in mice effectively lowered plasma triglycerides and improved glucose metabolism. This ANGPTL4 ASO treatment demonstrated a favorable safety profile in preclinical studies.

Area of Science:

  • Biochemistry
  • Pharmacology
  • Genetics

Background:

  • Angiopoietin-like 4 (ANGPTL4) is a key regulator of plasma triglyceride (TG) levels.
  • ANGPTL4 is a potential pharmacological target for managing dyslipidemia and cardiovascular disease.
  • Antisense oligonucleotides (ASOs) offer a method for gene silencing.

Purpose of the Study:

  • To investigate the efficacy of hepatocyte-targeting GalNAc-conjugated ASOs in silencing ANGPTL4 in mice.
  • To assess the impact of ANGPTL4 silencing on plasma lipid levels, glucose metabolism, and safety.

Main Methods:

  • Mice received ANGPTL4-targeting ASOs or control ASOs via injections.
  • Studies included short-term (2 weeks) and long-term (20 weeks) high-fat feeding protocols.
  • Measurements included ANGPTL4 levels, adipose LPL activity, plasma lipids, glucose, body weight, and safety markers.

Main Results:

  • ANGPTL4 ASOs significantly downregulated ANGPTL4 in liver and adipose tissue, increasing LPL activity and reducing plasma TGs.
  • Long-term treatment improved glucose tolerance, reduced food intake, and decreased weight gain.
  • No significant adverse effects such as lymphadenopathy or ascites were observed; liver enzymes remained normal.

Conclusions:

  • Hepatocyte-targeted ANGPTL4 ASOs are effective in reducing plasma TG levels in mice.
  • This therapeutic strategy shows a promising safety profile, suggesting potential for cardiovascular risk reduction.